Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema (Orphanet Journal of Rare Diseases, (2020), 15, 1, (221), 10.1186/s13023-020-01506-5)

Journal article published in 2021 by M. Magerl

, H. Gothe, S. Krupka, A. Lachmann, C. Ohlmeier

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